Data Foundry

Drug recalls 2017

Testosterone Cypionate 200 mg/mL — Class II drug recall D-0686-2017

Terminated recall by Isomeric Pharmacy Solution, LLC, reported 2017-05-03, distributed nationwide. Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of pro

Recall numberD-0686-2017
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmIsomeric Pharmacy Solution, LLC, Salt Lake City, UT, United States
Recall initiated2017-04-06
Classified2017-04-26
Reported by FDA2017-05-03
Terminated2017-08-30
DistributedNationwide (US)
Quantity2,156 vials
Reason classessterility
UPC / GTIN / UDI-DI00370285120039
Lot numbers09018, 09023, 09024, 09027, 09031, 10005, 10010, 11022, 11038, 11044, 12003, 12010, 12021
Model numbers1200
Expiration dates2017-04-17, 2017-04-22, 2017-04-23, 2017-04-25, 2017-04-30, 2017-05-06, 2017-05-09, 2017-06-10, 2017-06-18, 2017-07-04, 2017-07-08, 2017-07-12, 2017-07-30

Product

Testosterone Cypionate 200 mg/mL, Testosterone Propionate 20 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1200, barcode 3 70285 12003 9.

Reason for recall

Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0686-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.